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rs10985112

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs10985112(A;A)
Make rs10985112(A;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position120969130
GeneC5
is asnp
is mentioned by
dbSNPrs10985112
ebirs10985112
HLIrs10985112
Exacrs10985112
Varsomers10985112
Maprs10985112
PheGenIrs10985112
hapmaprs10985112
1000 genomesrs10985112
hgdprs10985112
ensemblrs10985112
gopubmedrs10985112
geneviewrs10985112
scholarrs10985112
googlers10985112
pharmgkbrs10985112
gwascentralrs10985112
openSNPrs10985112
23andMers10985112
23andMe allrs10985112
SNP Nexus

SNPshotrs10985112
SNPdbers10985112
MSV3drs10985112
GWAS Ctlgrs10985112
GMAF0.1552
Max Magnitude0
? (A;A) (A;G) (G;G) 28
Rs10985112
PubMed [PMID 17880261OA-icon.png]
Affy Probeset SNP_A-4241423
Affy Orientation same
On GW 5.0 1
Alleles A/B A/G
Ancestral A
Population Caucasian
Allele A
Case Freq. 0.1
Control Freq. 0.07
Odds Ratio Het
Odds Ratio Hom
Odds Ratio All 1.57
Disease Rheumatoid Arthritis (RA)


rs10985112 increases susceptibility to Rheumatoid Arthritis 1.57 times for carriers of the A allele [PMID 17880261OA-icon.png]

[PMID 20018075OA-icon.png] Genome-wide association study of rheumatoid arthritis by a score test based on wavelet transformation.